Beta-endorphin secretion by human peripheral blood mononuclear cells: regulation by glucocorticoids

Life Sci. 1990;46(17):1233-40. doi: 10.1016/0024-3205(90)90498-g.

Abstract

Corticotropin-releasing factor (CRF), a 41-aminoacid neuropeptide, can induce lymphocytes to production of beta-endorphin (beta E). Furthermore, the neuropeptide Arginine-Vasopressin (AVP) can enhance CRF-induced production of beta E. We have demonstrated that CRF acts by stimulating monocytes to production of the cytokine interleukin-1 (IL-1). IL-1 can in its turn activate the lymphocytes to secretion of beta E. Here we demonstrate that the glucocorticoid analogue dexamethasone is capable of modulating CRF-induced beta E secretion by lymphocytes. It appeared that dexamethasone can inhibit secretion of lymphocyte-derived beta E. The mechanism by which dexamethasone exerts its inhibitory activity is by blocking CRF-induced production of IL-1, thereby preventing induction of beta E secretion by B cells. These results support the concept that peptide hormones and glucocorticoids are mediating a reciprocal modulation of neuroendocrine and immunological activities.

MeSH terms

  • Arginine Vasopressin / physiology
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / metabolism*
  • Cells, Cultured
  • Corticotropin-Releasing Hormone / physiology
  • Dexamethasone
  • Glucocorticoids / physiology*
  • Humans
  • Interleukin-1 / biosynthesis
  • Monocytes / drug effects
  • Monocytes / physiology
  • Recombinant Proteins
  • beta-Endorphin / metabolism*

Substances

  • Glucocorticoids
  • Interleukin-1
  • Recombinant Proteins
  • Arginine Vasopressin
  • beta-Endorphin
  • Dexamethasone
  • Corticotropin-Releasing Hormone